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An efficient and stereoselective synthesis of platelet-activating factors and the enantiomers from D- and L- tartaric acids

Tetrahedron letters, 1982, Vol.23 (34), p.3507-3510

1982

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Cyclic pentapeptide endothelin antagonists with high ETA selectivity. Potency- and solubility-enhancing modifications

Journal of medicinal chemistry, 1992-05, Vol.35 (11), p.2139-2142

1992

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Antibody to Platelet Activating Factor (1-O-Alkyl-2-Acetyl-sn-Glycero-3-Phosphocholine; PAF)

Journal of biochemistry (Tokyo), 1987-09, Vol.102 (3), p.451-453

1987

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Structure-Activity Relationships of Cyclic Pentapeptide Endothelin A Receptor Antagonists

Journal of medicinal chemistry, 1995-10, Vol.38 (21), p.4309-4324

1995

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A Molecular Design toward Biologically Significant Compounds based on PAF Structures

Journal of Synthetic Organic Chemistry, Japan, 1987/04/01, Vol.45(4), pp.369-384

1987

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Nonpeptide mimetics of .beta.-turns: a facile oxidative intramolecular cycloaddition of an azodicarbonyl system

Journal of the American Chemical Society, 1988-03, Vol.110 (5), p.1638-1639

1988

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Synthesis and Biological Activity of Fluorine-Modified Platelet Activating Factors

Chemical and Pharmaceutical Bulletin, 1987/02/25, Vol.35(2), pp.647-653

1987

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Enantiospecific routes to 3,4 disubstituted azetidinones

Tetrahedron, 1991, Vol.47 (7), p.1137-1144

1991

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Linear peptide ETA antagonists: rational design and practical derivatization of N-terminal amino- and imino-carbonylated tripeptide derivatives

Bioorganic & medicinal chemistry letters, 1995-07, Vol.5 (13), p.1395-1400

1995

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Practical synthesis of a cyclic pentapeptide in solution : large-scale preparation of a representative ETA-selective antagonist, BQ-123Na

Bioorganic & medicinal chemistry letters, 1994-07, Vol.4 (13), p.1613-1618

1994

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Practical synthesis of a cyclic pentapeptide in solution: large-scale preparation of a representative ET A-selective antagonist, BQ-123Na

Bioorganic & medicinal chemistry letters, 1994-07, Vol.4 (13), p.1613-1618

1994

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Linear peptide ET A antagonists: rational design and practical derivatization of N-terminal amino- and imino-carbonylated tripeptide derivatives

Bioorganic & medicinal chemistry letters, 1995, Vol.5 (13), p.1395-1400

1995

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The design and synthesis of mimetics of peptide β-turns

Journal of molecular recognition, 1988-04, Vol.1 (2), p.75-79

1988

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Antibody to Platelet Activating Factor (1-O-Alkyl-2-Acetyl-sn-Glycero-3-Phosphocholine; PAF)1

Journal of biochemistry (Tokyo), 1987-09, Vol.102 (3), p.451-453

1987

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Molecular design toward biologically significant compounds based on platelet activating factor: a highly selective agonist as a potential antihypertensive agent

Journal of medicinal chemistry, 1986-10, Vol.29 (10), p.1812-1814

1986

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タンパクの部位特異的切断の新手法

ファルマシア, 1990/11/01, Vol.26(11), pp.1143

藤田, かがり

1990

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An Enantioselective Synthesis of Platelet-Activating Factors, Their Enantiomers, and Their Analogues from D-and L-Tartaric Acids

Chemical and Pharmaceutical Bulletin, 1985/02/25, Vol.33(2), pp.572-582

1985

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Lineage-specific expression of granulocyte colony-stimulating factor and thrombopoietin receptors in terminally differentiated hematopoietic cells

Experimental hematology, 2006-12, Vol.34 (12), p.1651-1654

2006

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An efficient and stereoselective synthesis of platelet-activating factors and the enantiomers from D- and L- tartaric acids

Cyclic pentapeptide endothelin antagonists with high ETA selectivity. Potency- and solubility-enhancing modifications

Antibody to Platelet Activating Factor (1-O-Alkyl-2-Acetyl-sn-Glycero-3-Phosphocholine; PAF)

Structure-Activity Relationships of Cyclic Pentapeptide Endothelin A Receptor Antagonists

A Molecular Design toward Biologically Significant Compounds based on PAF Structures

Nonpeptide mimetics of .beta.-turns: a facile oxidative intramolecular cycloaddition of an azodicarbonyl system

Synthesis and Biological Activity of Fluorine-Modified Platelet Activating Factors

Enantiospecific routes to 3,4 disubstituted azetidinones

Linear peptide ETA antagonists: rational design and practical derivatization of N-terminal amino- and imino-carbonylated tripeptide derivatives

Practical synthesis of a cyclic pentapeptide in solution : large-scale preparation of a representative ETA-selective antagonist, BQ-123Na

Practical synthesis of a cyclic pentapeptide in solution: large-scale preparation of a representative ET A-selective antagonist, BQ-123Na

Linear peptide ET A antagonists: rational design and practical derivatization of N-terminal amino- and imino-carbonylated tripeptide derivatives

The design and synthesis of mimetics of peptide β-turns

Antibody to Platelet Activating Factor (1-O-Alkyl-2-Acetyl-sn-Glycero-3-Phosphocholine; PAF)1

Molecular design toward biologically significant compounds based on platelet activating factor: a highly selective agonist as a potential antihypertensive agent

タンパクの部位特異的切断の新手法

An Enantioselective Synthesis of Platelet-Activating Factors, Their Enantiomers, and Their Analogues from D-and L-Tartaric Acids

Lineage-specific expression of granulocyte colony-stimulating factor and thrombopoietin receptors in terminally differentiated hematopoietic cells

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